CAS 26211-73-4

Methanone, (2-methyl-1H-indol-3-yl)phenyl-

Description:

Methanone, (2-methyl-1H-indol-3-yl)phenyl-, also known by its CAS number 26211-73-4, is an organic compound characterized by its indole and phenyl functional groups. This compound features a methanone functional group, which is indicative of a ketone structure, where a carbonyl group (C=O) is bonded to two carbon-containing groups. The presence of the 2-methyl-1H-indole moiety suggests that it has a bicyclic structure, contributing to its potential biological activity and aromatic properties. The phenyl group enhances its stability and may influence its reactivity and solubility in various solvents. This compound is likely to exhibit interesting chemical behavior due to the conjugation between the indole and phenyl rings, which can affect its electronic properties. Additionally, its structural features may allow for interactions with biological targets, making it of interest in medicinal chemistry and drug development. Overall, the compound's unique structure and functional groups contribute to its potential applications in various fields, including pharmaceuticals and organic synthesis.

Formula: C₁₆H₁₃NO

3-Benzoyl-2-methyl-1H-indole

Controlled Product

CAS: 26211-73-4

3-Benzoyl-2-methyl-1H-indole is an isomer of tetrahydrocarbazole. It has a high yield and optical purity. 3-Benzoyl-2-methyl-1H indole can be synthesized from β-unsaturated aldehydes, such as 2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2yl)-3,5,6,-trimethylphenol. The compound has been shown to react with alkali metals to form a salt in the presence of dehydrogenative conditions. This reaction proceeds via an iminium intermediate that reacts with the metal salt to produce the product. 3BzIMeI can also react with alcohols or amines in the presence of heterocycles such as mesitylene to form substituted benzimidazoles.

Formula: C₁₆H₁₃NO

Purity: Min. 95%

Molecular weight: 235.28 g/mol

Ref: 3D-BBA21173